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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472547Generated: October 30, 2026

Isatoic Anhydride → 2-Amino-N-methoxybenzamide

https://huagongshe.com/reaction/1472547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsatoic AnhydrideHCID 8359—
ReactantTriethylamineHCID 8471—
ReactantWater ethanolHCID 19096565—
Product2-Amino-N-methoxybenzamideHCID 1239270749%

Reaction Steps

To a mixture of isatoic anhydride (40 g, 245.39 mmol, 1 eq) and o-methyl hyroxylamine hydrochloride (30.55 g, 368.09 mmole, 1.5 eq) in EtOH:H2O (9:1) (1000 mL) was added triethylamine (51.2 mL, 368.09 mmole, 1.5 eq) and resulting mixture was reflux for 4 h. After completion of reaction solvent was removed under reduced pressure and residue was diluted with water (500 mL), extracted with ethyl acetate (3×250 mL). Combined organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. Solid compound so obtained was purified by washing with diethyl ether and hexane to give the title compound as brown solid (20 g, 49%). 1H-NMR (400 MHz, DMSO-d6): δ 3.67 (s, 3H), 6.20-6.40 (brs, 2H), 6.44-6.53 (m, 1H), 6.70 (d, 1H, J=7.76 Hz), 7.10-7.19 (m, 1H), 7.30 (d, 1H, J=7.6 Hz), 11.40 (s, 1H). LC-MS [M+H]+=167.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012479B2
Source datasetuspto-grants-2015_04
ORD IDord-c416878864c2497ba88c6da76d9ba63f
Source noteuspto-grants-2015_04